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(4-Chlorophenyl)(2-methoxybenzylidene)azane oxide, also known as 4-Chloro-2-methoxybenzylideneamino oxide, is an azane oxide derivative with a molecular formula of C14H12ClNO2. It is a white to off-white powder that has potential applications in the pharmaceutical industry and as a reagent in organic synthesis. (4-Chlorophenyl)(2-methoxybenzylidene)azane oxide has been studied for its potential biological activities, such as being a potential anticonvulsant and anti-inflammatory agent. It is crucial to handle (4-Chlorophenyl)(2-methoxybenzylidene)azane oxide with care due to its potential hazardous properties and to follow proper safety protocols when working with it in a laboratory or industrial setting.

19865-62-4

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19865-62-4 Usage

Uses

Used in Pharmaceutical Industry:
(4-Chlorophenyl)(2-methoxybenzylidene)azane oxide is used as a potential therapeutic agent for its potential anticonvulsant and anti-inflammatory properties. Its application in this industry is due to its biological activities that may help in the treatment of various conditions related to seizures and inflammation.
Used in Organic Synthesis:
(4-Chlorophenyl)(2-methoxybenzylidene)azane oxide is used as a reagent in organic synthesis for its ability to contribute to the formation of complex molecular structures. Its application in this industry is due to its chemical properties that facilitate the synthesis of other compounds with potential applications in various fields.

Check Digit Verification of cas no

The CAS Registry Mumber 19865-62-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,8,6 and 5 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 19865-62:
(7*1)+(6*9)+(5*8)+(4*6)+(3*5)+(2*6)+(1*2)=154
154 % 10 = 4
So 19865-62-4 is a valid CAS Registry Number.

19865-62-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(4-chlorophenyl)-1-(2-methoxyphenyl)methanimine oxide

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:19865-62-4 SDS

19865-62-4Downstream Products

19865-62-4Relevant academic research and scientific papers

Synthesis and Evaluation of Novel 5-cyclohexyl-2-(4″-substitutedphenyl)-3-(2″-substitutedphenyl)4H-2,3,3a,5,6,6a-hexahydropyrrolo[3,4-d]isoxazole-4,6-dione Derivatives for Their In Vitro Antioxidant and Antibacterial Activities

Kaur, Manpreet,Kaur, Anjandeep,Singh, Baldev,Singh, Baljit

, p. 80 - 88 (2017)

1,3-Dipolar cycloaddition reactions of N-cyclohexyl maleimide (1) with azomethine N-oxide (2) have afforded novel isoxazolidine (3) in excellent yield. Their structures have been characterized from their IR,1H-NMR,13C-NMR,1H,1H-COSY, MS(ESI), and elemental analysis techniques. In vitro antibacterial activity of the synthesized compounds were investigated against a representative panel of pathogenic strains specifically two Gram-positive bacteria (Staphylococcus aureus and Streptococcus pyogenes) and two Gram-negative bacteria (Pseudomonas aeruginosa and Escherichia coli) using agar-well diffusion assay. Some of the compounds (3a, 3k, 3n, and 3o) exhibited promising antibacterial activities. All the synthesized compounds have also been screened for their antioxidant activities and were found to be significantly active.

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